Canonical Allele Identifier: CA1281312535

Gene: DPP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.115753241G= , CM000664.2:g.115753241G=	GRCh38
NC_000002.11:g.116510817G= , CM000664.1:g.116510817G=	GRCh37
NC_000002.10:g.116227287G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410059.6:c.1018G= MANE Select	ENSP00000386565.1:p.Ala340=
ENST00000310323.12:c.997G=	ENSP00000309066.8:p.Ala333=
ENST00000393147.6:c.1030G=	ENSP00000376855.2:p.Ala344=
ENST00000409163.5:c.868G=	ENSP00000387038.1:p.Ala290=
ENST00000410059.5:c.1018G=	ENSP00000386565.1:p.Ala340=
NM_001004360.3:c.997G=	NP_001004360.2:p.Ala333=
NM_001178034.1:c.1030G=	NP_001171505.1:p.Ala344=
NM_001178036.1:c.868G=	NP_001171507.1:p.Ala290=
NM_001178037.1:c.1006G=	NP_001171508.1:p.Ala336=
NM_020868.3:c.1018G=	NP_065919.2:p.Ala340=
XM_011511526.1:c.997G=	XP_011509828.1:p.Ala333=
XM_011511527.1:c.868G=	XP_011509829.1:p.Ala290=
XM_011511528.1:c.766G=	XP_011509830.1:p.Ala256=
XR_923234.1:n.67+1494C=
NM_001321905.1:c.1069G=	NP_001308834.1:p.Ala357=
NM_001321906.1:c.997G=	NP_001308835.1:p.Ala333=
NM_001321907.1:c.1018G=	NP_001308836.1:p.Ala340=
NM_001321908.1:c.928G=	NP_001308837.1:p.Ala310=
NM_001321909.1:c.901G=	NP_001308838.1:p.Ala301=
NM_001321910.1:c.868G=	NP_001308839.1:p.Ala290=
NM_001321911.1:c.868G=	NP_001308840.1:p.Ala290=
NM_001321912.1:c.868G=	NP_001308841.1:p.Ala290=
NM_001321913.1:c.256G=	NP_001308842.1:p.Ala86=
NM_001321914.1:c.256G=	NP_001308843.1:p.Ala86=
NM_020868.4:c.1018G=	NP_065919.2:p.Ala340=
XM_017004566.1:c.895G=	XP_016860055.1:p.Ala299=
XM_024453023.1:c.997G=	XP_024308791.1:p.Ala333=
XR_923234.2:n.67+1494C=
NM_001004360.4:c.997G=	NP_001004360.3:p.Ala333=
NM_001178036.2:c.868G=	NP_001171507.2:p.Ala290=
NM_001178037.2:c.1006G=	NP_001171508.2:p.Ala336=
NM_001321905.2:c.1069G=	NP_001308834.2:p.Ala357=
NM_001321907.2:c.1018G=	NP_001308836.2:p.Ala340=
NM_001321908.2:c.928G=	NP_001308837.2:p.Ala310=
NM_001321909.2:c.901G=	NP_001308838.2:p.Ala301=
NM_001321910.2:c.868G=	NP_001308839.2:p.Ala290=
NM_001321911.2:c.868G=	NP_001308840.2:p.Ala290=
NM_001321912.2:c.868G=	NP_001308841.2:p.Ala290=
NM_001321913.2:c.256G=	NP_001308842.2:p.Ala86=
NM_020868.6:c.1018G= MANE Select	NP_065919.3:p.Ala340=
NM_001004360.5:c.997G=	NP_001004360.3:p.Ala333=
NM_001178036.3:c.868G=	NP_001171507.2:p.Ala290=
NM_001178037.3:c.1006G=	NP_001171508.2:p.Ala336=
NM_001321905.3:c.1069G=	NP_001308834.2:p.Ala357=
NM_001321906.2:c.997G=	NP_001308835.2:p.Ala333=
NM_001321907.3:c.1018G=	NP_001308836.2:p.Ala340=
NM_001321908.3:c.928G=	NP_001308837.2:p.Ala310=
NM_001321909.3:c.901G=	NP_001308838.2:p.Ala301=
NM_001321910.3:c.868G=	NP_001308839.2:p.Ala290=
NM_001321911.3:c.868G=	NP_001308840.2:p.Ala290=
NM_001321912.3:c.868G=	NP_001308841.2:p.Ala290=
NM_001321913.3:c.256G=	NP_001308842.2:p.Ala86=
NM_001321914.2:c.256G=	NP_001308843.2:p.Ala86=
NM_001399849.1:c.868G=	NP_001386778.1:p.Ala290=
NM_001399850.1:c.256G=	NP_001386779.1:p.Ala86=
NM_001399851.1:c.766G=	NP_001386780.1:p.Ala256=